Epilepsy with bilateral occipital Calcifications: A benign onset with progressive severity

G. Gobbi; G. Sorrenti; M. Santucci; P. Giovanardi Rossi; P. Ambrosetto; R. Michelucci; C. A. Tassinari

Epilepsy with bilateral occipital Calcifications: A benign onset with progressive severity

G. Gobbi, G. Sorrenti, M. Santucci, P. Giovanardi Rossi, P. Ambrosetto, R. Michelucci, C. A. Tassinari

Istituto Scienze Neurologiche

Research output: Contribution to journal › Article › peer-review

Abstract

We studied four patients with a focal epilepsy and bilateral occipital corticosubcortical calcifications without any sign of phakomatosis. The clinical course of the disease was similar in all the patients and evolved from a benign onset to a severe encephalopathy with progressive mental impairment. The question of whether these patients have an incomplete and atypical form of Sturge-Weber syndrome or a previously undescribed disorder is addressed.

Original language	English
Pages (from-to)	913-920
Number of pages	8
Journal	Neurology
Volume	38
Issue number	6
Publication status	Published - 1988

ASJC Scopus subject areas

Arts and Humanities (miscellaneous)
Clinical Neurology
Neuroscience(all)

Cite this

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abstract = "We studied four patients with a focal epilepsy and bilateral occipital corticosubcortical calcifications without any sign of phakomatosis. The clinical course of the disease was similar in all the patients and evolved from a benign onset to a severe encephalopathy with progressive mental impairment. The question of whether these patients have an incomplete and atypical form of Sturge-Weber syndrome or a previously undescribed disorder is addressed.",

author = "G. Gobbi and G. Sorrenti and M. Santucci and {Giovanardi Rossi}, P. and P. Ambrosetto and R. Michelucci and Tassinari, {C. A.}",

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AU - Gobbi, G.

AU - Sorrenti, G.

AU - Santucci, M.

AU - Giovanardi Rossi, P.

AU - Ambrosetto, P.

AU - Michelucci, R.

AU - Tassinari, C. A.

PY - 1988

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AB - We studied four patients with a focal epilepsy and bilateral occipital corticosubcortical calcifications without any sign of phakomatosis. The clinical course of the disease was similar in all the patients and evolved from a benign onset to a severe encephalopathy with progressive mental impairment. The question of whether these patients have an incomplete and atypical form of Sturge-Weber syndrome or a previously undescribed disorder is addressed.

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Epilepsy with bilateral occipital Calcifications: A benign onset with progressive severity

Abstract

ASJC Scopus subject areas

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